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Volumn 31, Issue 13, 1990, Pages 1833-1836

Preparation and reactivity of β-zinc and copper phosphonates

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHONIC ACID DERIVATIVE;

EID: 0025239877     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)98798-7     Document Type: Article
Times cited : (31)

References (42)
  • 16
    • 84989444996 scopus 로고
    • Synthesis and Wittig-Horner Reactions of 1-(Functionally)Substituted 2,2-Dimethylpropanephosphonic Esters (1-t-Butyl-substituted Phosphonic Esters)
    • (1983) Synthesis , pp. 449
    • Schaumann1    Fittkau2
  • 18
    • 84914379636 scopus 로고    scopus 로고
    • The zinc dust used was purchased from Aldrich (-325 mesh).
  • 19
    • 84914379635 scopus 로고    scopus 로고
    • The polar phosphonate group considerably accelerates the rate of formation of the zinc organometallic (non-functionalized alkyl bromides usually cannot be converted to the corresponding organozinc compounds in THF).
  • 20
    • 0000399484 scopus 로고
    • We reported recently that β-cyano zinc and copper organometallics also do not eliminate the cyano group at temperature below 30°C see:
    • (1988) Tetrahedron Lett. , vol.29 , pp. 2395
    • Yeh1    Knochel2
  • 37
    • 84914379634 scopus 로고    scopus 로고
    • 2 group by a dimethyl pentylphosphonate group) during the reaction of2c to β-nitrostyrene if this reaction is performed at 0 °C.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.